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Viral Infection Study

Effect of short term inhaled Budesonide in children with mild COVID 19 infection an open labeled randomized controlled trial - NA

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/06/034327
Enrollment
150
Registered
2021-06-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere

Interventions

Intervention1: Budesonide 400 mcg: twice daily for 7 days Control Intervention1: Standard of Care: Vitamin C and zinc supplements once daily for 14 days

Sponsors

Apollo Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Confirmed diagnosis of COVID 19 infection(COVID RT-PCR positive or HRCT suggestive of CORADS 4/5/6) Mild disease presenting within the first 7 days of illness

Exclusion criteria

Exclusion criteria: Children with moderate or severe COVID 19 infection at presentation. Children with comorbidities on immunosuppressants or on steroids. Parents or guardian not consenting to be part of the study.

Design outcomes

Primary

MeasureTime frame
Effect on disease progression in children affected with COVID 19Timepoint: 14 days

Secondary

MeasureTime frame
Effect on symptom controlTimepoint: 14 days

Countries

India

Contacts

Public ContactDr Ayesha Mariam

Apollo Childrenâ??s Hospital

ayesha.mariam@yahoo.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026